FDA Inspection 1201241 — Ajinomoto Omnichem NV

Ajinomoto Omnichem NV — FEI 3002807802

The FDA completed an inspection of Ajinomoto Omnichem NV on March 16, 2022 in Wetteren. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 16, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wetteren (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)